Product Details

SNP ID
rs141889164
Assay Type
Functionally tested
NCBI dbSNP Submissions
12
Location
Chr.1:115286243 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAATGCCCCGGCACCCGCTGTCAA[C/T]GGGATTTGGGTCCCGGCACTTGGTC
Phenotype
MIM: 162030
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NGF PubMed Links

Gene Details

Gene
NGF
Gene Name
nerve growth factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002506.2 722 Missense Mutation ATT,GTT I185V NP_002497.2
XM_006710663.3 722 Missense Mutation ATT,GTT I185V XP_006710726.1
XM_011541518.2 722 Missense Mutation ATT,GTT I240V XP_011539820.1

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